GRIM-19:调节抗肿瘤和先天免疫反应的双刃剑

Translational oncogenomics Pub Date : 2008-03-17
Shreeram C Nallar, Sudhakar Kalakonda, Peng Sun, Dhan V Kalvakolanu
{"title":"GRIM-19:调节抗肿瘤和先天免疫反应的双刃剑","authors":"Shreeram C Nallar,&nbsp;Sudhakar Kalakonda,&nbsp;Peng Sun,&nbsp;Dhan V Kalvakolanu","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Gene associated with retinoid-interferon-β-induced mortality (GRIM)-19, was originally identified as a critical regulatory protein necessary for Interferon-β-Retinoic acid-induced cell death. Overexpression of GRIM-19 activates cell death and its suppression or inactivation promotes cell growth. GRIM-19 targets multiple proteins/pathways for exerting growth control and cell death. However, GRIM-19 is also required for normal cellular processes. In addition, viruses 'hijack' GRIM-19 for their survival. Intracellular bacterial infections and bacterial products have been reported to induce the expression of GRIM-19. In this review, we will discuss the current status of GRIM-19 in growth control and innate immune response.</p>","PeriodicalId":88783,"journal":{"name":"Translational oncogenomics","volume":"3 ","pages":"67-79"},"PeriodicalIF":0.0000,"publicationDate":"2008-03-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3022361/pdf/","citationCount":"0","resultStr":"{\"title\":\"GRIM-19: A Double-edged Sword that Regulates Anti-Tumor and Innate Immune Responses.\",\"authors\":\"Shreeram C Nallar,&nbsp;Sudhakar Kalakonda,&nbsp;Peng Sun,&nbsp;Dhan V Kalvakolanu\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Gene associated with retinoid-interferon-β-induced mortality (GRIM)-19, was originally identified as a critical regulatory protein necessary for Interferon-β-Retinoic acid-induced cell death. Overexpression of GRIM-19 activates cell death and its suppression or inactivation promotes cell growth. GRIM-19 targets multiple proteins/pathways for exerting growth control and cell death. However, GRIM-19 is also required for normal cellular processes. In addition, viruses 'hijack' GRIM-19 for their survival. Intracellular bacterial infections and bacterial products have been reported to induce the expression of GRIM-19. In this review, we will discuss the current status of GRIM-19 in growth control and innate immune response.</p>\",\"PeriodicalId\":88783,\"journal\":{\"name\":\"Translational oncogenomics\",\"volume\":\"3 \",\"pages\":\"67-79\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2008-03-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3022361/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Translational oncogenomics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Translational oncogenomics","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

与类视黄素-干扰素-β诱导死亡(GRIM)相关的基因19最初被确定为干扰素-β-视黄酸诱导细胞死亡所必需的关键调控蛋白。GRIM-19过表达可激活细胞死亡,抑制或失活可促进细胞生长。GRIM-19靶向多种蛋白/途径,发挥生长控制和细胞死亡。然而,正常的细胞过程也需要GRIM-19。此外,病毒为了生存“劫持”了GRIM-19。细胞内细菌感染和细菌产物可诱导GRIM-19的表达。在这篇综述中,我们将讨论GRIM-19在生长控制和先天免疫应答中的研究现状。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

摘要图片

摘要图片

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
GRIM-19: A Double-edged Sword that Regulates Anti-Tumor and Innate Immune Responses.

Gene associated with retinoid-interferon-β-induced mortality (GRIM)-19, was originally identified as a critical regulatory protein necessary for Interferon-β-Retinoic acid-induced cell death. Overexpression of GRIM-19 activates cell death and its suppression or inactivation promotes cell growth. GRIM-19 targets multiple proteins/pathways for exerting growth control and cell death. However, GRIM-19 is also required for normal cellular processes. In addition, viruses 'hijack' GRIM-19 for their survival. Intracellular bacterial infections and bacterial products have been reported to induce the expression of GRIM-19. In this review, we will discuss the current status of GRIM-19 in growth control and innate immune response.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Advances in Sarcoma Genomics and Therapeutic Management Single Nucleotide Polymorphisms in Cancer Research and Treatment Rationale for Immunotherapy in Gastrointestinal Malignancies Proteomics Profiling of Pancreatic Cancer Molecular Pathways in Melanomagenesis
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1